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Cross-architecture tuning of silicon and SiGe-based quantum devices using machine learning.

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Nanostructured 3C-SiC on Si by a network of (111) platelets: a fully textured film generated by intrinsic growth anisotropy.

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TRPML1 links lysosomal calcium to autophagosome biogenesis through the activation of the CaMKKβ/VPS34 pathway.

Nature communications·2019

Voltage-tunable dual-band Ge/Si photodetector operating in VIS and NIR spectral range.

Optics express·2019

Ultra-wideband Ge-rich silicon germanium mid-infrared polarization rotator with mode hybridization flattening.

Optics express·2019

Steroid therapy in an alpha-dystroglycanopathy due to GMPPB gene mutations: A case report.

Neuromuscular disorders : NMD·2018

Rate and Shape of Functional Decline in Amyotrophic Lateral Sclerosis Identify Clinically Distinct Amyotrophic Lateral Sclerosis Phenotypes.

Annals of neurology·2026

Ambulatory Episodic Hypertension in Parkinson's Disease With Orthostatic Hypotension.

Annals of neurology·2026

Accelerated Epigenetic Aging in Frontotemporal Dementia Highlights Smoking, Inflammation, and Metabolic Signals.

Annals of neurology·2026

A Recurrent 3'UTR Variant in CAPN3 Highlights the Diagnostic Impact of Non-Coding Variants in Limb-Girdle Muscular Dystrophies.

Annals of neurology·2026

Salivary Dim-Light Melatonin Onset is Associated with Functional Decline, Respiratory Symptom Emergence, and Survival in Early Amyotrophic Lateral Sclerosis.

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Hemispheric Asymmetry of Neuroimaging Biomarkers in Early Onset Alzheimer's Disease: Clinical and Cognitive Outcomes.

Annals of neurology·2026

A Time-Course Transcriptomic Resource for Early Embryogenesis in Lethenteron reissneri.

International journal of molecular sciences·2026

Genetic Architecture and Biological Mechanisms of Adolescent Idiopathic Scoliosis: From Susceptibility Loci to Functional Pathways.

Journal of clinical medicine·2026

Twins Discordant for Parkinson's Disease: A 10-Year Longitudinal Follow-Up of Mortality, Clinical and Lifestyle Features, Nutritional Status, and Dietary Habits.

Brain sciences·2026

SLC52A2-Related Riboflavin Transporter Deficiency in Non-Isolated Auditory Neuropathy: Evidence from a Chinese Cohort and a Global Variant Review.

Genes·2026

Novel Compound Heterozygous CEP152 Variants Associated with Atypical Seckel Syndrome 5 in a Chinese Child: Functional Characterization of a Novel Splice-Site Variant and Expansion of the Genotype-Phenotype Spectrum.

Genes·2026

Assembly of a high-quality reference genome for the rat tapeworm Hymenolepis diminuta.

G3 (Bethesda, Md.)·2026

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X-linked ichthyosis due to steroid sulfatase deficiency associated with hypogonadism and anosmia

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